Arjo, Inc. Recalls
9 recalls on record · July 18, 2012 to July 19, 2017 · Medical Devices
Recalls by year
12
13
14
16
17
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 19, 2017Medical DevicesFDA
Arjo, Inc. dba ArjoHuntleigh recalls ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein Thro
Hazard: Reports of the device failure involving delivering continuous pressure to the calf garment and not deflating as intended, without triggering an alarm.
April 20, 2016Medical DevicesFDA
Arjo, Inc. dba ArjoHuntleigh recalls The Concerto Basic Shower Trolley is intended for assisted hygiene care, especially showering and bathing of residents i
Hazard: Reports of the bolts connecting the stretcher to the hydraulic piston and the stretcher tilting mechanism becoming loose.
October 22, 2014Medical DevicesFDA
Arjo, Inc. dba ArjoHuntleigh recalls Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling Lift; Mode
Hazard: The upper portion of the hooks on the spreader bar are too flexible for holding the loops of the sling. The loop of the sling could potentially come out of the hooks if positioned in the upper portion of the hooks.
August 14, 2013Medical DevicesFDA
Arjo, Inc. dba ArjoHuntleigh recalls Enterprise 9000 Bed; an AC-powered adjustable hospital bed with built-in electronic weigh scale, patient bed exit alarm,
Hazard: ArjoHuntleigh has received reports of unintended movement where the backrest and/or thigh sections of the bed have moved without anyone consciously pressing the control button. These incidents have occurred in High Dependency and Intensive Therapy environments where unintended movement of the patient may have serious consequences.
August 14, 2013Medical DevicesFDA
Arjo, Inc. dba ArjoHuntleigh recalls Enterprise 8000 Bed; an AC-powered adjustable hospital bed; ArjoHuntleigh AB, Eslov, Sweden; Models 8000, 8001, 8002, 80
Hazard: ArjoHuntleigh has received reports of unintended movement where the backrest and/or thigh sections of the bed have moved without anyone consciously pressing the control button. These incidents have occurred in High Dependency and Intensive Therapy environments where unintended movement of the patient may have serious consequences.
January 2, 2013Medical DevicesFDA
Arjo, Inc. dba ArjoHuntleigh recalls Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov, Swe
Hazard: The Flowtron Trio DVT Pump has been marketed without proper FDA Approval.
July 18, 2012Medical DevicesFDA
Arjo, Inc. dba ArjoHuntleigh recalls Sara Plus Mobile Patient Lifter; manufactured for Arjo by Medibo Medical Products N.V., Heikant 5, B-3930 Hamont-Achel,
Hazard: ArjoHuntleigh has received a limited number of customer reports concerning injuries related to an exposed metal support bracket when the proactive knee pad assembly is removed.
July 18, 2012Medical DevicesFDA
Arjo, Inc. dba ArjoHuntleigh recalls Chorus Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Model
Hazard: ArjoHuntleigh has received a limited number of customer reports concerning injuries related to an exposed metal support bracket when the proactive knee pad assembly is removed.
July 18, 2012Medical DevicesFDA
Arjo, Inc. dba ArjoHuntleigh recalls Encore Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Model
Hazard: ArjoHuntleigh has received a limited number of customer reports concerning injuries related to an exposed metal support bracket when the proactive knee pad assembly is removed.